A study comparing the effect of two pain reducing methods namely quadratus lumborum block and transversus abdominis plane block in decreasing pain in patients operated for total laparoscopic hysterectomy by comparing total dose of pain reducing drugs consumed by patients after surgery.

A comparative study of Quadratus Lumborum block and Transversus Abdominis Plane block for postoperative analgesia in patients undergoing Total Laparoscopic Hysterectomy-A Prospective Randomized Controlled Trial - nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/11/097070

Enrollment

Registered

2025-11-07

Start date

Unknown

Completion date

Unknown

Last updated

2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: 1- Obstetrics

Interventions

Intervention1: Quadratus Lumborum block: Patients operated for Total Laparoscopic Hysterectomy will be divided into two groups A and B. Group B will be administered Quadratus Lumborum block with 20 ml

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient scheduled for elective Total Laparoscopic Hysterectomy. 2. ASA physical status 1 and 2. 3. Age from 35 to 60 years. 4. Willing to give informed/written consent.

Exclusion criteria

Exclusion criteria: 1. History of known allergy to drugs used in study. 2. Coagulopathy or patient on anticoagulant therapy. 3. ASA physical status 3 and 4. 4. Local infection. 5. BMI more than 35 kilogram per metre square. 6. Presence of psychiatric illness.

Design outcomes

Primary

Measure	Time frame
Total tramadol(analgesic) consumption in 24 hours post surgery.Timepoint: Total tramadol(analgesic) consumption in 24 hours post surgery.	—

Secondary

Measure	Time frame
Effect on intraoperative hemodynamics.Timepoint: ;Intra-operative fentanyl consumption.Timepoint: ;Pain score(VAS) 0 to 10Timepoint: at baseline;Time to first analgesic in post operative period.Timepoint: ;Post operative complicationsTimepoint: ;To assess patient satisfaction scores regarding pain management in 24 hours postoperatively.Timepoint:	—

Countries

India

Contacts

Public ContactBachitar Singh

Livasa Hospital, Mohali

drbijaypgimer@gmail.com7986692323

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026